Create issue ticket

127 Possible Causes for Mutation in the Thyroid Hormone Receptor Interactor 11 Gene, Often Stillborn

  • Achondrogenesis Type 1B

    The outcome is most often very poor.[medlineplus.gov] In mice, a nonsense mutation in the thyroid hormone receptor interactor 11 gene (Trip11), which encodes the Golgi microtubule-associated protein 210 (GMAP-210), resulted in[en.wikipedia.org] Outlook (Prognosis) The outcome is most often very poor.[huronregional.org]

  • Achondrogenesis

    The outcome is most often very poor.[nlm.nih.gov] In mice, a nonsense mutation in the thyroid hormone receptor interactor 11 gene (Trip11), which encodes the Golgi microtubule-associated protein 210 (GMAP-210), resulted in[en.wikipedia.org] A nonsense mutation in the thyroid hormone receptor interactor 11 gene (Trip11), which encodes the Golgi microtubule-associated protein 210 (GMAP-210), showed defects that[symptoma.com]

  • Achondrogenesis, Type 1A

    The outcome is most often very poor.[medlineplus.gov] In mice, a nonsense mutation in the thyroid hormone receptor interactor 11 gene (Trip11), which encodes the Golgi microtubule-associated protein 210 (GMAP-210), resulted in[dict.eudic.net] Outlook (Prognosis) The outcome is most often very poor.[huronregional.org]

  • Atelosteogenesis Type 2

    It is often confused with diastrophic dysplasia owing to similar symptoms.[onlymyhealth.com] In mice, a nonsense mutation in the thyroid hormone receptor interactor 11 gene (Trip11), which encodes the Golgi microtubule-associated protein 210 (GMAP-210), resulted in[drsherazi110.blogspot.com] Those with the disorder are usually stillborn. The disorder is extremely rare and is caused by mutations in the SLC26A2 gene.[onlymyhealth.com]

  • Birth

    They started to prepare us for one of the biggest ordeals any woman could face – birthing their stillborn child.[theguardian.com] It was explained that in these circumstances the process was often quick and that we should consider how we might feel when our daughter was born.[theguardian.com]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene
  • Toxoplasmosis

    The damage to the unborn child is often more severe the earlier in pregnancy the transmission occurs.[web.archive.org] Potential results can be A miscarriage A stillborn child A child born with signs of congenital toxoplasmosis (e.g., abnormal enlargement or smallness of the head) Infants[cdc.gov] Potential results can be a miscarriage a stillborn child a child born with signs of toxoplasmosis (e.g., abnormal enlargement or smallness of the head) Infants infected before[web.archive.org]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene
  • Temporal Lobe Epilepsy

    His mother married at the age of 31, had a stillborn first son, and 1 year later gave birth to Vincent. Vincent was a moody child, self-willed, and often annoying.[oadoi.org]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene
  • Malignant Angioendotheliomatosis

    Two cases have been reported in the literature occurring in a stillborn infant and in an adolescent man. 5 6 The clinical picture is often characterized by a fever of unknown[nature.com]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene
  • Spinal Trauma

    They most often involve the cervical spine, followed by the cervical-thoracic junction, and thoracolumbar junction.[journals.lww.com] […] influencing outcome is a delay in diagnosis and treatment. 22,32 Neonatal Injuries Birth-related injuries to the spine are rare; however, one study 35 found that 10% of stillborn[journals.lww.com]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene
  • Amelia of Lower Limb

    Affected infants are often stillborn or die shortly after birth. [1] Description [ edit ] Amelia may be present as an isolated defect, but it is often associated with major[en.wikipedia.org]

    Missing: Mutation in the Thyroid Hormone Receptor Interactor 11 Gene

Further symptoms